- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06314360
Comparison of Foot Posture, Plantar Pressure, and Postural Balance in Patellofemoral Pain Patients and Healthy Subjects
Comparison of Foot Posture, Plantar Pressure, and Postural Balance in Individuals With Patellofemoral Pain and Healthy Individuals
Patellofemoral pain syndrome (PFS) is a musculoskeletal problem characterized by pain felt in the front of the knee or behind the patella, commonly affecting individuals in adolescence or young adulthood, especially those engaged in sports such as cycling and running. It is one of the most encountered knee injuries and can have a poor prognosis. The intensity of knee pain increases during functional activities such as stair climbing, squatting, running, and jumping due to the increased patellofemoral joint reaction force.
A disturbance in postural stability is observed in individuals with PFS due to pain during functional activities. Studies examining changes in foot posture, plantar pressure, and postural balance in individuals with PFS are quite limited and controversial. Moreover, research that simultaneously investigates these parameters and interprets the results is scarce. Some studies have utilized detailed technical systems such as medical imaging or motion analysis, while practical methods incorporating foot posture and plantar pressure analyses are available and easy to use in clinical settings.
There is a lack of literature on the easy assessment and interpretation of plantar pressure, postural balance, and functional activities in individuals with PFS. Within the scope of this project, the plan is to assess plantar pressure, postural balance, and functional activities in individuals with PFS. The aim is to quickly interpret the biomechanical changes occurring in these individuals and guide rehabilitation programs based on the obtained data.
The use of practical and fast assessment methods in planning treatments for PFS is crucial for early rehabilitation planning. Practical methods such as foot posture, plantar pressure, and postural balance assessments, which can be used in clinical settings, may provide benefits in shaping rehabilitation goals related to lower extremity alignment in individuals with PFS. The objective of this study is to compare the foot posture, plantar pressure, and postural stability of individuals with PFS with healthy individuals. Additionally, the investigators aim to investigate the relationship between foot posture, plantar pressure parameters, postural balance, and functional level in individuals with PFS. Through these objectives, it will be possible to identify potential parameters that could be effective in rehabilitation processes and contribute to determining treatment programs by revealing biomechanical changes in individuals with PFS.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
PFS, commonly referred to as pain felt in the front or behind the kneecap, is a prevalent lower extremity problem. It most commonly affects adolescents and young adults, especially those engaged in sports such as cycling and running. Although its etiology is not fully explained, factors such as increased load on anatomical structures, repetitive movements with excessive degrees of knee flexion, patellofemoral malalignment, and muscle strength losses contribute to the pain. PFS is a frequently encountered musculoskeletal problem that adversely affects the quality of life and functional status in young adults.
Changes in lower extremity alignment (dynamic valgus, varus, tibial rotation, etc.) and alterations in foot position (increased pronation posture) are among the most important factors leading to PFS. Increased foot pronation during ground contact in walking and in static standing is suggested to trigger the development of PFS. Studies have shown that increased force and pressure distribution in the medial forefoot, midfoot, and heel after long-distance runs are associated with PFS. Conversely, there are studies suggesting no difference in foot posture between individuals with PFS and healthy individuals. One method that can be preferred to assess foot posture (in static or dynamic positions) is the measurement of plantar pressure distribution. This measurement method, based on plantar pressure distribution, is described as a safe and non-invasive method that allows the examination of changes related to the locomotor system, especially foot biomechanics. There are also systems that assess foot pressure distribution concurrently with evaluating foot position. Studies in the literature have demonstrated an association between foot pronation and increased plantar pressure in the medial foot in individuals with PFS. Additionally, there are studies indicating that the distribution of plantar pressure is similar between individuals with PFS and healthy individuals or that foot pronation is less in individuals with PFS compared to healthy individuals. Therefore, a clear conclusion in the literature regarding the foot plantar pressure in individuals with PFS has not yet been reached.
The severity of pain in PFS increases not only during daily life activities such as climbing stairs, squatting, and standing up from sitting but also during sports activities such as running and jumping. Studies show that during activities where weight is transferred to a single extremity, such as single-leg squatting, individuals with PFS experience decreased hip flexion, increased hip adduction and internal rotation, and disrupted pelvic alignment. It is suggested that if pelvic alignment cannot be maintained during weight transfer, postural balance will be negatively affected. The number of studies examining postural balance in individuals with PFS is limited, and a consensus has not been reached.
The evaluation methods used in the aforementioned studies generally rely on radiological imaging or motion analysis systems. Only a limited number of studies have utilized foot posture assessment and plantar pressure analysis. The different assessment methods used make it difficult to draw clear relationships between the results. Therefore, there is a need for a comprehensive study that evaluates parameters such as foot posture, plantar pressure, postural balance, and functional status together in individuals with PFS.
The use of practical and fast assessment methods is crucial in planning treatments for PFS to enable early rehabilitation planning. Therefore, practical methods such as foot posture, plantar pressure distribution, and postural balance assessments, which can be used in clinical settings, may provide benefits in shaping rehabilitation goals related to lower extremity alignment in individuals with PFS. The aim of this study is to compare the foot posture, plantar pressure distribution, and postural balance parameters of individuals with PFS with healthy individuals and to investigate the relationship between these parameters in individuals with PFS.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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Ankara/Sıhhıye
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Ankara, Ankara/Sıhhıye, Turkey, 06100
- Hacettepe University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion criteria for individuals with PFS:
- Those who have been experiencing pain for at least 6 months
- Those who met the numerical pain criteria, defined as a minimum of 3 out of 10 points
- Having pain in the activities specifically identified as painful for PFP patients, including prolonged sitting, descending and ascending stairs/slopes, squatting, running, and jumping.
Inclusion criteria for healthy individuals:
- Those who are without any complaints related to the lower extremities in the last 6 months
- Those who have not undergone lower extremity surgery for any reason
- Those who do not have a diagnosis of neurological or orthopedic diseases
Exclusion criteria for individuals with PFS:
- Those with a history of lower extremity injury in the last 6 months
- Those who had patellofemoral dislocation and/or subluxation
- Those with meniscus and ligament lesions, bone anomalies
- Those who have undergone surgery on any lower extremity joint (hip, knee, or ankle)
Exclusion criteria for healthy individuals:
- Those with a history of lower extremity injury in the last 6 months
- Those who are asymptomatic with a history of patellofemoral dislocation and/or subluxation
- Those who are asymptomatic with meniscus and ligament lesions, bone anomalies
- Those who have undergone lower extremity surgery
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Subjects with Patellofemoral Pain
Demographic data, pain information, limb dominancy will be collected.
Then, functional status will be assessed with Kujala Patellofemoral Pain Form; foot posture will be evaluated with Foot Posture Index; plantar pressure and postural balance values will be collected with the K-Invent K-Plates device.
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There is no intervention in this study.
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Healthy Control Subjects
Demographic data, limb dominancy will be collected.
Then, functional status will be assessed with Kujala Patellofemoral Pain Form; foot posture will be evaluated with Foot Posture Index; plantar pressure and postural balance values will be collected with the K-Invent K-Plates device.
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There is no intervention in this study.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Plantar Pressure
Time Frame: 3 minutes, in the baseline assessment session.
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Plantar pressure assessment will be performed with K-Invent K-Plates device.
This device has two separate platforms measuring 320x160 mm.
Participants will stand on the device with each foot on a platform and pressure data will be collected as max kg and weigth distribution.
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3 minutes, in the baseline assessment session.
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Postural Stability
Time Frame: 20 minutes, in the baseline assessment session.
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Postural stability assessment will be performed with K-Invent K-Plates device.
This device has two separate platforms measuring 320x160 mm.
While the participants are on the device with each foot on a platform, bipodal and then unipodal stance data will be collected respectively.
Data will be collected three times for 50 seconds for each stance and stability data such as center of pressure, velocity and ellipse area will be recorded.
Higher values show poor balance scores.
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20 minutes, in the baseline assessment session.
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Foot posture
Time Frame: 5 minutes, in the baseline assessment session.
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Foot Posture Index will be used to evaluate foot posture.
FPI is a six-item clinical assessment tool used to evaluate foot posture.
The six criteria used in the evaluation are talar head palpation, supra malleolar and infra malleolar curvature, position of the calcaneal in the frontal plane, protrusion in the talonavicular joint region, compliance of the medial longitudinal arch, and abduction/adduction of the forefoot.
Each API component is scored from -2 to +2, with -2 representing clear signs of supination and +2 indicating positive signs of pronation.
The total score ranges from -12 to +12.
Total scores between 0 and +5 indicate normal/neutral foot posture.
Values ≥ +6 are considered pronated foot, while values below 0 are considered supinated foot.
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5 minutes, in the baseline assessment session.
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Functionality
Time Frame: 3 minutes, in the baseline assessment session.
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Functional status will be assessed using Kujala Patellofemoral Pain Form.
The questionnare consists of 13 questions.
These questions ask whether there is pain during going up and down stairs, squatting, running, jumping and sitting for long periods with the knees flexed; It evaluates whether there is limp, swelling or subluxation of the patella, the amount of atrophy in the quadriceps muscle, flexion deficit and the need for a walking aid.
The scoring system ranges from 0-100 points, from worst to best.
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3 minutes, in the baseline assessment session.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain Assessment
Time Frame: 1 minute, in the baseline assessment session.
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Pain will be evaluated using Numeric Analogue Scale.
In this scale, the intensity of pain at the time of questioning will be recorded by the person choosing the value corresponding to the relevant number on a 10 cm long line shown between 0 (no pain) and 10 (unbearable pain).
Two separate inquiries will be made, including pain at rest and during activity.
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1 minute, in the baseline assessment session.
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Limb dominance
Time Frame: 30 seconds, in the baseline assessment session.
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Limb dominance will be recorded by asking "Which leg do you prefer to kick a ball?".
The answer to this question will be recorded as the dominant leg.
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30 seconds, in the baseline assessment session.
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Hande Guney, Hacettepe University Faculty of Physical Therapy and Rehabilitation
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BAP_PFS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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